A method for designing a protein capable of binding in an RNA base selective manner or RNA base sequence specific manner is provided. The protein of the present invention is a protein containing one or more of PPR motifs (preferably 2 to 14 PPR motifs) each consisting of a polypeptide of 30- to 38-amino acid length represented by the formula 1 (wherein Helix A is a moiety of 12-amino acid length capable of forming an α-helix structure, and is represented by the formula 2, wherein, in the formula 2, A1 to A12 independently represent an amino acid; X does not exist, or is a moiety of 1- to 9-amino acid length; Helix B is a moiety of 11- to 13-amino acid length capable of forming an α-helix structure; and L is a moiety of 2- to 7-amino acid length represented by the formula 3, wherein, in the formula 3, the amino acids are numbered “i” (-1), “ii” (-2), and so on from the C-terminus side, provided that Liii to Lvii may not exist), and combination of three amino acids A1, A4 and Lii, or combination of two amino acids A4, and Lii is a combination corresponding to a target RNA base or base sequence.
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2. The method according to claim 1 , wherein the combination of the three amino acids A 1 , A 4 and L ii is determined according to any one of the following propositions: (3-1) when the three amino acids A 1 , A 4 , and L ii are valine, asparagine, and aspartic acid, respectively, the PPR motif can selectively bind to U (uracil); (3-2) when the three amino acids A 1 , A 4 , and L ii are valine, threonine, and asparagine, respectively, the PPR motif can selectively bind to A (adenine); (3-3) when the three amino acids A 1 , A 4 , and L ii are valine, asparagine, and asparagine, respectively, the PPR motif can selectively bind to C (cytosine); (3-4) when the three amino acids A 1 , A 4 , and L ii are glutamic acid, glycine, and aspartic acid, respectively, the PPR motif can selectively bind to G (guanine); (3-5) when the three amino acids A 1 , A 4 , and L ii are isoleucine, asparagine, and asparagine, respectively, the PPR motif can selectively bind to C or U; (3-6) when the three amino acids A 1 , A 4 , and L ii are valine, threonine, and aspartic acid, respectively, the PPR motif can selectively bind to G; (3-7) when the three amino acids A 1 , A 4 , and L ii are lysine, threonine, and aspartic acid, respectively, the PPR motif can selectively bind to G; (3-8) when the three amino acids A 1 , A 4 , and L ii are phenylalanine, serine, and asparagine, respectively, the PPR motif can selectively bind to A; (3-9) when the three amino acids A 1 , A 4 , and L ii are valine, asparagine, and serine, respectively, the PPR motif can selectively bind to C; (3-10) when the three amino acids A 1 , A 4 , and L ii are phenylalanine, threonine, and asparagine, respectively, the PPR motif can selectively bind to A; (3-11) when the three amino acids A 1 , A 4 , and L ii are isoleucine, asparagine, and aspartic acid, respectively, the PPR motif can selectively bind to U or A; (3-12) when the three amino acids A 1 , A 4 , and L ii are threonine, threonine, and asparagine, respectively, the PPR motif can selectively bind to A; (3-13) when the three amino acids A 1 , A 4 , and L ii are isoleucine, methionine, and aspartic acid, respectively, the PPR motif can selectively bind to U or C; (3-14) when the three amino acids A 1 , A 4 , and L ii are phenylalanine, proline, and aspartic acid, respectively, the PPR motif can selectively bind to U; (3-15) when the three amino acids A 1 , A 4 , and L ii are tyrosine, proline, and aspartic acid, respectively, the PPR motif can selectively bind to U; and (3-16) when the three amino acids A 1 , A 4 , and L ii are leucine, threonine, and aspartic acid, respectively, the PPR motif can selectively bind to G.
3. The method according to claim 1 , wherein the combination of the two amino acids A 4 and L ii is determined according to any one of the following propositions: (2-1) when A 4 and L ii are asparagine and aspartic acid, respectively, the motif can selectively bind to U; (2-2) when A 4 and L ii are asparagine and asparagine, respectively, the motif can selectively bind to C; (2-3) when A 4 and L ii are threonine and asparagine, respectively, the motif can selectively bind to A; (2-4) when A 4 and L ii are threonine and aspartic acid, respectively, the motif can selectively bind to G; (2-5) when A 4 and L ii are serine and asparagine, respectively, the motif can selectively bind to A; (2-6) when A 4 and L ii are glycine and aspartic acid, respectively, the motif can selectively bind to G; (2-7) when A 4 and L ii are asparagine and serine, respectively, the motif can selectively bind to C; (2-8) when A 4 and L ii are proline and aspartic acid, respectively, the motif can selectively bind to U; (2-9) when A 4 and L ii are glycine and asparagine, respectively, the motif can selectively bind to A; (2-10) when A 4 and L ii are methionine and aspartic acid, respectively, the motif can selectively bind to U; (2-11) when A 4 and L ii are leucine and aspartic acid, respectively, the motif can selectively bind to C; and (2-12) when A 4 and L ii are valine and threonine, respectively, the motif can selectively bind to U.
4. A method for controlling a function of RNA, comprising: preparing a complex comprising a protein region consisting of a protein obtained by the method according to claim 1 , linked to a functional region; preparing a cell containing an RNA having a target sequence; and introducing the complex into the cell, whereby the protein region of the complex binds to the RNA having the target sequence and the functional region modifies the function of the RNA.
5. A complex comprising a region consisting of a protein prepared by the method according to claim 1 , linked to a functional region.
6. A method for modifying a cellular genetic material, which comprises the following steps: preparing a cell containing an RNA having a target sequence; and introducing the complex according to claim 5 into the cell, whereby the protein region of the complex binds to the RNA having the target sequence, and the functional region modifies the target sequence.
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October 22, 2012
December 6, 2016
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